ATE399012T1 - CARBAMINIC ACID DERIVATIVES CONTAINING A PIPERAZINE LINKAGE AS HDAC INHIBITORS - Google Patents
CARBAMINIC ACID DERIVATIVES CONTAINING A PIPERAZINE LINKAGE AS HDAC INHIBITORSInfo
- Publication number
- ATE399012T1 ATE399012T1 AT03722719T AT03722719T ATE399012T1 AT E399012 T1 ATE399012 T1 AT E399012T1 AT 03722719 T AT03722719 T AT 03722719T AT 03722719 T AT03722719 T AT 03722719T AT E399012 T1 ATE399012 T1 AT E399012T1
- Authority
- AT
- Austria
- Prior art keywords
- acid derivatives
- hdac inhibitors
- derivatives containing
- carbaminic acid
- hdac
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
- C07D295/26—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/60—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyridine Compounds (AREA)
- Indole Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Abstract
This invention pertains to certain carbamic acid compounds which inhibit HDAC (histone deacetylase) activity of the following formula: The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit HDAC, and in the treatment of conditions mediated by HDAC, cancer, proliferative conditions, psoriasis, etc.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US36933702P | 2002-04-03 | 2002-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE399012T1 true ATE399012T1 (en) | 2008-07-15 |
Family
ID=28675576
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT03722719T ATE399012T1 (en) | 2002-04-03 | 2003-04-03 | CARBAMINIC ACID DERIVATIVES CONTAINING A PIPERAZINE LINKAGE AS HDAC INHIBITORS |
Country Status (13)
Country | Link |
---|---|
US (3) | US7629343B2 (en) |
EP (1) | EP1492534B1 (en) |
JP (1) | JP4606027B2 (en) |
AT (1) | ATE399012T1 (en) |
AU (1) | AU2003229883B2 (en) |
BR (1) | BR0308908A (en) |
CA (1) | CA2479906C (en) |
DE (1) | DE60321775D1 (en) |
ES (1) | ES2309313T3 (en) |
MX (1) | MXPA04009490A (en) |
NO (1) | NO329942B1 (en) |
NZ (1) | NZ536116A (en) |
WO (1) | WO2003082288A1 (en) |
Families Citing this family (70)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7517884B2 (en) | 1998-03-30 | 2009-04-14 | Kalypsys Inc. | Sulfonyl-substituted bicyclic compounds as modulators of PPAR |
ATE398105T1 (en) | 2002-03-13 | 2008-07-15 | Janssen Pharmaceutica Nv | CARBONYLAMINO DERIVATIVES AS NEW INHIBITORS OF HISTONE DEACETYLASE |
MXPA04007776A (en) | 2002-03-13 | 2004-10-15 | Janssen Pharmaceutica Nv | Sulfonylamino-derivatives as novel inhibitors of histone deacetylase. |
EA007272B1 (en) | 2002-03-13 | 2006-08-25 | Янссен Фармацевтика Н. В. | New inhibitors of histone deacetylase |
BR0307606A (en) | 2002-03-13 | 2004-12-21 | Janssen Pharmaceutica Nv | Piperazinyl, piperidinyl and morpholinyl derivatives as histone deacetylase inhibitors |
ATE399012T1 (en) * | 2002-04-03 | 2008-07-15 | Topotarget Uk Ltd | CARBAMINIC ACID DERIVATIVES CONTAINING A PIPERAZINE LINKAGE AS HDAC INHIBITORS |
TW200418806A (en) | 2003-01-13 | 2004-10-01 | Fujisawa Pharmaceutical Co | HDAC inhibitor |
US7652036B2 (en) | 2003-02-25 | 2010-01-26 | Topotarget Uk Limited | Carbamic acid compounds comprising a bicyclic heteroaryl group as HDAC inhibitors |
JP2007512367A (en) * | 2003-11-26 | 2007-05-17 | エートン ファーマ インコーポレーティッド | Diamine and iminodiacetic acid hydroxamic acid derivatives |
GB0401876D0 (en) | 2004-01-28 | 2004-03-03 | Vereniging Het Nl Kanker I | New use for cancer antigen |
US7534918B2 (en) * | 2004-07-12 | 2009-05-19 | Merck & Co., Inc. | Histone deacetylase inhibitors |
SG156687A1 (en) | 2004-07-28 | 2009-11-26 | Janssen Pharmaceutica Nv | Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase |
ME01058B (en) | 2004-07-28 | 2012-10-20 | Janssen Pharmaceutica Nv | Substituted propenyl piperazine derivatives as novel inhibitors of histone deacetylase |
DE602005014646D1 (en) * | 2004-07-28 | 2009-07-09 | Janssen Pharmaceutica Nv | SUBSTITUTED PROPENYLPIPERAZINE DERIVATIVES AS NEW INHIBITORS OF HISTONDEACETYLASE |
GB2417682A (en) * | 2004-08-18 | 2006-03-08 | Univ East Anglia | Histone deacetylse inhibitor for treating connective tissue disorders |
AU2005307006B2 (en) | 2004-10-29 | 2012-05-03 | Kalypsys, Inc. | Sulfonyl-substituted bicyclic compounds as modulators of PPAR |
JPWO2006082834A1 (en) * | 2005-02-02 | 2008-06-26 | 興和株式会社 | Prophylactic / therapeutic agent for diseases caused by keratinocyte proliferation |
ITFI20050041A1 (en) * | 2005-03-15 | 2006-09-16 | Menarini Internat Operations Luxembourg Sa | HYDROXAMMED AS INHIBITORS OF ISTONE DEACELITASIS, THEIR PREPARATION AND PHARMACEUTICAL FORMULATIONS THAT CONTAIN THEM |
GB0509225D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Inhibitors of enzymatic activity |
GB0509223D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Enzyme inhibitors |
DK1901729T3 (en) | 2005-05-13 | 2012-05-14 | Topotarget Uk Ltd | Pharmaceutical formulations of HDAC inhibitors |
EP1885710B1 (en) | 2005-05-18 | 2015-08-19 | Janssen Pharmaceutica N.V. | Substituted aminopropenyl piperidine or morpholine derivatives as novel inhibitors of histone deacetylase |
AU2006270322A1 (en) | 2005-07-14 | 2007-01-25 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
CA2620333A1 (en) | 2005-08-26 | 2007-03-01 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
AR058065A1 (en) * | 2005-09-27 | 2008-01-23 | Novartis Ag | CARBOXYAMINE COMPOUNDS AND USE OF THE SAME PHARMACEUTICAL COMPOSITIONS. |
US20070088043A1 (en) * | 2005-10-18 | 2007-04-19 | Orchid Research Laboratories Limited. | Novel HDAC inhibitors |
EP1940389A2 (en) | 2005-10-21 | 2008-07-09 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
NZ566831A (en) | 2005-10-25 | 2011-09-30 | Kalypsys Inc | Salts of modulators of PPAR and methods of treating metabolic disorders |
ATE509920T1 (en) | 2005-10-27 | 2011-06-15 | Janssen Pharmaceutica Nv | SQUARE ACID DERIVATIVES AS INHIBITORS OF HISTONE DEACETYLASE |
CA2625210A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
CA2627923C (en) | 2005-11-10 | 2016-01-12 | Topotarget Uk Limited | Histone deacetylase (hdac) inhibitors (pxdlol) for the treatment of cancer |
WO2007070506A2 (en) | 2005-12-14 | 2007-06-21 | Amgen Inc. | Diaza heterocyclic sulfonamide derivatives and their uses |
CN101370803B (en) | 2006-01-19 | 2012-12-12 | 詹森药业有限公司 | Substituted indolyl-alkyl-amino-derivatives as inhibitors of histone deacetylase |
EP1979328B1 (en) | 2006-01-19 | 2012-12-26 | Janssen Pharmaceutica N.V. | Pyridine and pyrimidine derivatives as inhibitors of histone deacetylase |
JP5247470B2 (en) | 2006-01-19 | 2013-07-24 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Pyridine and pyrimidine derivatives as inhibitors of histone deacetylase |
CN101374828B (en) | 2006-01-19 | 2012-09-19 | 詹森药业有限公司 | Heterocyclylalkyl derivatives as novel inhibitors of histone deacetylase |
US8101616B2 (en) | 2006-01-19 | 2012-01-24 | Janssen Pharmaceutica N.V. | Pyridine and pyrimidine derivatives as inhibitors of histone deacetylase |
JP5225104B2 (en) | 2006-01-19 | 2013-07-03 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Aminophenyl derivatives as new inhibitors of histone deacetylase |
MX2008010035A (en) | 2006-02-07 | 2008-10-17 | Astellas Pharma Inc | N-hydroxyacrylamide compounds. |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
MX2008014320A (en) | 2006-05-09 | 2009-03-25 | Braincells Inc | 5 ht receptor mediated neurogenesis. |
MX2009002496A (en) | 2006-09-08 | 2009-07-10 | Braincells Inc | Combinations containing a 4-acylaminopyridine derivative. |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
GB0619753D0 (en) | 2006-10-06 | 2006-11-15 | Chroma Therapeutics Ltd | Enzyme inhibitors |
WO2008053131A1 (en) | 2006-10-30 | 2008-05-08 | Chroma Therapeutics Ltd. | Hydroxamates as inhibitors of histone deacetylase |
US20080176861A1 (en) | 2007-01-23 | 2008-07-24 | Kalypsys, Inc. | Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis |
MX2010003230A (en) | 2007-09-25 | 2010-04-07 | Topotarget Uk Ltd | Methods of synthesis of certain hydroxamic acid compounds. |
CN101970399A (en) | 2007-12-14 | 2011-02-09 | 乔治敦大学 | Histone deacetylase inhibitors |
JP5564033B2 (en) | 2008-03-27 | 2014-07-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Aza-bicyclohexyl substituted indolylalkylamino derivatives as novel inhibitors of histone deacetylase |
WO2010001366A1 (en) * | 2008-07-04 | 2010-01-07 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Piperazines derivatives as proteasome modulators |
US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
GB0903480D0 (en) | 2009-02-27 | 2009-04-08 | Chroma Therapeutics Ltd | Enzyme Inhibitors |
WO2011153359A1 (en) | 2010-06-04 | 2011-12-08 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
US8609672B2 (en) | 2010-08-27 | 2013-12-17 | University Of The Pacific | Piperazinylpyrimidine analogues as protein kinase inhibitors |
WO2012087889A2 (en) * | 2010-12-20 | 2012-06-28 | The Ohio State University Research Foundation | Dna methylation inhibitors |
CN102260225B (en) * | 2011-06-02 | 2013-08-21 | 蒋杰 | Phenylpiperazine derivatives for inhibiting tumor metastasis and tumor angiogenesis |
WO2013066831A1 (en) * | 2011-10-31 | 2013-05-10 | Glaxosmithkline Llc | Compounds and methods |
CN104136410A (en) * | 2011-12-29 | 2014-11-05 | 药品循环公司 | Cinnamic acid hydroxyamides as inhibitors of histone deacetylase 8 |
SG10201802911RA (en) | 2013-03-15 | 2018-05-30 | Global Blood Therapeutics Inc | Compounds and uses thereof for the modulation of hemoglobin |
WO2015058106A1 (en) * | 2013-10-18 | 2015-04-23 | The General Hospital Corporation | Imaging histone deacetylases with a radiotracer using positron emission tomography |
EA201992707A1 (en) | 2013-11-18 | 2020-06-30 | Глобал Блад Терапьютикс, Инк. | COMPOUNDS AND THEIR APPLICATIONS FOR HEMOGLOBIN MODULATION |
ES2694053T3 (en) * | 2014-03-12 | 2018-12-17 | Chong Kun Dang Pharmaceutical Corp. | Novel compounds as inhibitors of histone deacetylase 6 and pharmaceutical compositions comprising the same |
US10478431B2 (en) | 2014-11-26 | 2019-11-19 | The J. David Gladstone Institutes | Methods for treating a cytomegalovirus infection |
US9745253B2 (en) | 2015-03-13 | 2017-08-29 | Forma Therapeutics, Inc. | Alpha-cinnamide compounds and compositions as HDAC8 inhibitors |
NZ736015A (en) | 2015-05-22 | 2019-04-26 | Chong Kun Dang Pharmaceutical Corp | Heterocyclicalkyl derivative compounds as selective histone deacetylase inhibitors and pharmaceutical compositions comprising the same |
WO2018165520A1 (en) | 2017-03-10 | 2018-09-13 | Vps-3, Inc. | Metalloenzyme inhibitor compounds |
US20220154282A1 (en) | 2019-03-12 | 2022-05-19 | The Broad Institute, Inc. | Detection means, compositions and methods for modulating synovial sarcoma cells |
KR20230134547A (en) * | 2021-01-20 | 2023-09-21 | 라이톡스 리미티드 | Protected histone deacetylase (HDAC) inhibitors |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5318964A (en) | 1992-06-11 | 1994-06-07 | Hoffmann-La Roche Inc. | Hydroxamic derivatives and pharmaceutical compositions |
JPH0775593A (en) * | 1993-09-08 | 1995-03-20 | Suntory Ltd | Production of protein |
JPH07278086A (en) * | 1993-11-08 | 1995-10-24 | Terumo Corp | Hydroxamic acid derivative and medicinal preparation containing the same |
GB9501737D0 (en) | 1994-04-25 | 1995-03-22 | Hoffmann La Roche | Hydroxamic acid derivatives |
EP0827742A1 (en) | 1996-09-04 | 1998-03-11 | Vrije Universiteit Brussel | Use of histone deacetylase inhibitors for treating fribosis or cirrhosis |
JP3563411B2 (en) * | 1997-01-23 | 2004-09-08 | エフ・ホフマン−ラ ロシュ アーゲー | Sulfamide-metalloprotease inhibitors |
DE69819878T2 (en) * | 1997-03-04 | 2004-04-22 | Monsanto Co. | DIVALENT SULFONYL-ARYL OR HETEROARYL HYDROXAMIC ACID COMPOUNDS |
US7115632B1 (en) * | 1999-05-12 | 2006-10-03 | G. D. Searle & Co. | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
US6696449B2 (en) * | 1997-03-04 | 2004-02-24 | Pharmacia Corporation | Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors |
AU8858398A (en) | 1997-07-10 | 1999-02-08 | Pharmacia & Upjohn S.P.A. | Matrix metalloproteinase inhibitors |
PL340551A1 (en) | 1997-11-12 | 2001-02-12 | Darwin Discovery Ltd | Derivatives of hydroxamic and carboxylic acids exhibiting mmp & tnf inhibitive action |
CZ2001126A3 (en) * | 1998-07-21 | 2002-01-16 | Warner-Lambert Company | Coadministration of ACAT and MMP inhibitors for the treatment of atherosclerotic lesions |
EP1107953A1 (en) | 1998-08-29 | 2001-06-20 | British Biotech Pharmaceuticals Limited | Hydroxamic acid derivatives as proteinase inhibitors |
GB9919776D0 (en) | 1998-08-31 | 1999-10-27 | Zeneca Ltd | Compoujnds |
US6492394B1 (en) * | 1998-12-22 | 2002-12-10 | Syntex (U.S.A.) Llc | Sulfonamide hydroxamates |
CZ20012294A3 (en) | 1998-12-22 | 2001-12-12 | F. Hoffmann-La Roche Ag | Sulfonamide hydroxamates |
US6448250B1 (en) | 1999-02-08 | 2002-09-10 | G. D. Searle & Company | Sulfamato hydroxamic acid metalloprotease inhibitor |
JP2003525203A (en) * | 1999-03-22 | 2003-08-26 | ダーウィン・ディスカバリー・リミテッド | Hydroxam and carboxylic acid derivatives |
GB9911073D0 (en) | 1999-05-12 | 1999-07-14 | Darwin Discovery Ltd | Hydroxamic and carboxylic acid derivatives |
BR0011291A (en) * | 1999-05-12 | 2002-05-14 | Searle & Co | Hydroxamic acid derivatives as matrix metalloprotease inhibitors |
EP1202968A2 (en) | 1999-08-10 | 2002-05-08 | British Biotech Pharmaceuticals Limited | Antibacterial agents |
KR20020070285A (en) * | 1999-11-23 | 2002-09-05 | 메틸진, 인크. | Inhibitors of histone deacetylase |
AU2268401A (en) * | 1999-12-17 | 2001-06-25 | Versicor Inc | Novel succinate compounds, compositions and methods of use and preparation |
GB9929979D0 (en) | 1999-12-17 | 2000-02-09 | Darwin Discovery Ltd | Hydroxamic acid derivatives |
US6852752B2 (en) * | 1999-12-17 | 2005-02-08 | Vicuron Pharmaceuticals Inc. | Urea compounds, compositions and methods of use and preparation |
US6797820B2 (en) * | 1999-12-17 | 2004-09-28 | Vicuron Pharmaceuticals Inc. | Succinate compounds, compositions and methods of use and preparation |
US6495677B1 (en) * | 2000-02-15 | 2002-12-17 | Kanda S. Ramasamy | Nucleoside compounds |
WO2001062751A1 (en) | 2000-02-21 | 2001-08-30 | Astrazeneca Ab | Arylpiperazines and arylpiperidines and their use as metalloproteinase inhibiting agents |
ES2208595T3 (en) | 2000-05-15 | 2004-06-16 | Darwin Discovery Limited | DERIVATIVES OF HYDROXAMIC ACID. |
PE20020354A1 (en) | 2000-09-01 | 2002-06-12 | Novartis Ag | HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS |
WO2002028829A2 (en) | 2000-09-25 | 2002-04-11 | Questcor Pharmaceuticals, Inc. | Peptide deformylase inhibitors |
EP1328510B1 (en) | 2000-09-29 | 2013-11-20 | TopoTarget UK Limited | (e)-n-hydroxy-3-(3-sulfamoyl-phenyl)-acrylamide compounds and their therapeutic use |
GB0023983D0 (en) | 2000-09-29 | 2000-11-15 | Prolifix Ltd | Therapeutic compounds |
EP1335898B1 (en) | 2000-09-29 | 2005-11-23 | TopoTarget UK Limited | Carbamic acid compounds comprising an amide linkage as hdac inhibitors |
US6784173B2 (en) * | 2001-06-15 | 2004-08-31 | Hoffmann-La Roche Inc. | Aromatic dicarboxylic acid derivatives |
US6683078B2 (en) * | 2001-07-19 | 2004-01-27 | Pharmacia Corporation | Use of sulfonyl aryl or heteroaryl hydroxamic acids and derivatives thereof as aggrecanase inhibitors |
ATE399012T1 (en) * | 2002-04-03 | 2008-07-15 | Topotarget Uk Ltd | CARBAMINIC ACID DERIVATIVES CONTAINING A PIPERAZINE LINKAGE AS HDAC INHIBITORS |
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2003
- 2003-04-03 AT AT03722719T patent/ATE399012T1/en not_active IP Right Cessation
- 2003-04-03 ES ES03722719T patent/ES2309313T3/en not_active Expired - Lifetime
- 2003-04-03 AU AU2003229883A patent/AU2003229883B2/en not_active Ceased
- 2003-04-03 CA CA2479906A patent/CA2479906C/en not_active Expired - Fee Related
- 2003-04-03 EP EP03722719A patent/EP1492534B1/en not_active Expired - Lifetime
- 2003-04-03 US US10/509,732 patent/US7629343B2/en not_active Expired - Fee Related
- 2003-04-03 MX MXPA04009490A patent/MXPA04009490A/en active IP Right Grant
- 2003-04-03 BR BR0308908-8A patent/BR0308908A/en not_active IP Right Cessation
- 2003-04-03 JP JP2003579825A patent/JP4606027B2/en not_active Expired - Fee Related
- 2003-04-03 WO PCT/GB2003/001463 patent/WO2003082288A1/en active IP Right Grant
- 2003-04-03 NZ NZ536116A patent/NZ536116A/en not_active IP Right Cessation
- 2003-04-03 DE DE60321775T patent/DE60321775D1/en not_active Expired - Lifetime
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2004
- 2004-11-02 NO NO20044744A patent/NO329942B1/en not_active IP Right Cessation
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2008
- 2008-07-01 US US12/165,686 patent/US7981895B2/en not_active Expired - Lifetime
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2011
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US20050143385A1 (en) | 2005-06-30 |
NO20044744L (en) | 2004-11-02 |
CA2479906A1 (en) | 2003-10-09 |
JP2005527556A (en) | 2005-09-15 |
DE60321775D1 (en) | 2008-08-07 |
US7981895B2 (en) | 2011-07-19 |
JP4606027B2 (en) | 2011-01-05 |
AU2003229883A1 (en) | 2003-10-13 |
BR0308908A (en) | 2005-01-04 |
ES2309313T3 (en) | 2008-12-16 |
EP1492534B1 (en) | 2008-06-25 |
MXPA04009490A (en) | 2005-06-08 |
NZ536116A (en) | 2007-01-26 |
US20110275810A1 (en) | 2011-11-10 |
AU2003229883B2 (en) | 2009-06-11 |
US20080269237A1 (en) | 2008-10-30 |
WO2003082288A1 (en) | 2003-10-09 |
CA2479906C (en) | 2011-02-08 |
NO329942B1 (en) | 2011-01-24 |
EP1492534A1 (en) | 2005-01-05 |
US7629343B2 (en) | 2009-12-08 |
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